Deletion | NM_000157.4(GBA1):c.1265_1319del (p.Leu422fs) | GBA1 | Pathogenic | 1 | 155205541 | 155205595 | GGGACTGTCGACAAAGTTACGCACCCAATTGGGTCCTCCTTCGGGGTTCAGGGCAA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA253083,dbVar:nssv3761540,OMIM:606463.0023 |
single nucleotide variant | NM_000157.4(GBA1):c.1312G>A (p.Asp438Asn) | GBA1 | Pathogenic | 1 | 155205548 | 155205548 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA342713229 |
single nucleotide variant | NM_000157.4(GBA1):c.1297G>T (p.Val433Leu) | GBA1 | Pathogenic/Likely pathogenic | 1 | 155205563 | 155205563 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA253059,UniProtKB:P04062#VAR_003310,OMIM:606463.0005 |
single nucleotide variant | NM_000157.4(GBA1):c.1279G>T (p.Glu427Ter) | GBA1 | Likely pathogenic | 1 | 155205581 | 155205581 | C | A | criteria provided, single submitter | ClinGen:CA342713575 |
single nucleotide variant | NM_000157.4(GBA1):c.1271T>C (p.Leu424Pro) | GBA1 | Likely pathogenic | 1 | 155205589 | 155205589 | A | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000157.4(GBA1):c.1250G>A (p.Trp417Ter) | GBA1 | Likely pathogenic | 1 | 155205610 | 155205610 | C | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000157.4(GBA1):c.1246G>A (p.Gly416Ser) | GBA1 | Pathogenic/Likely pathogenic | 1 | 155205614 | 155205614 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA253107,UniProtKB:P04062#VAR_003303,OMIM:606463.0040 |
single nucleotide variant | NM_000157.4(GBA1):c.1240G>T (p.Val414Leu) | GBA1 | Pathogenic/Likely pathogenic | 1 | 155205620 | 155205620 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA221390,UniProtKB:P04062#VAR_010068 |
single nucleotide variant | NM_000157.4(GBA1):c.1208G>C (p.Ser403Thr) | GBA1 | Likely pathogenic | 1 | 155206052 | 155206052 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA253096,UniProtKB:P04062#VAR_003300,OMIM:606463.0032 |
single nucleotide variant | NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) | GBA1 | Pathogenic | 1 | 155206068 | 155206068 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA221386,OMIM:606463.0038 |